has material basis in germline mutation in RTN4IP1 optic atrophy 10 with or without ataxia, intellectual disability, and seizures https://github.com/monarch-initiative/mondo/issues/7951 https://www.malacards.org/card/optic_atrophy_10 https://www.malacards.org/card/optic_atrophy_10_with_or_without_ataxia_impaired_intellectual_development_and_seizures OPA10 MONDO:0020737 GARD:0018200 OMIM:616732 MEDGEN:905727 UMLS:C4225227 RTN4IP1-related optic atrophy with or without neurological features optic atrophy 10 with or without ataxia, mental retardation, and seizures DOID:0111434 RTN4IP1-optic atrophy 10 with or without ataxia, impaired intellectual development and seizures An optic atrophy caused by a variation in the RTN4IP1; the optic atrophy can be associated with neurological involvement, including intellectual disability, ataxia, seizures. hereditary optic atrophy